FDA 510(k) clearance · back to tracker

Ablation Confirmation

Neuwave Medical, Inc. cleared K150313 on 2015-07-09, decision: substantially equivalent

K-number

K150313

Sponsor

Neuwave Medical, Inc.

Device

Ablation Confirmation

Class

Class II

Decision

Substantially Equivalent

Decision date

2015-07-09

Product code

LLZ

Advisory committee

Radiology

Medical specialty

Radiology

Regulation number

892.2050

Official FDA record

Open K150313on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

Use this as a predicate

Drop K150313 into Compass and start a substantial-equivalence draft.

Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

Try the sandbox

Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.